Interplay between protein synthesis and degradation in the CNS: physiological and pathological implications

被引:45
作者
Ding, Qunxing
Cecarini, Valentina
Keller, Jeffrey N. [1 ]
机构
[1] Univ Kentucky, Dept Anat & Neurobiol, Lexington, KY 40506 USA
[2] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40536 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.tins.2006.11.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Compromise of the ubiquitin-proteasome system (UPS) is a potential basis for multiple physiological abnormalities and pathologies in the CNS. This could be because reduced protein turnover leads to bulk intracellular protein accumulation. However, conditions associated with compromised UPS function are also associated with impairments in protein synthesis, and impairment of UPS function is sufficient to inhibit protein synthesis. These data suggest that the toxicity of UPS inhibition need not depend on gross intracellular protein accumulation, and indicate the potential for crosstalk between the UPS and protein-synthesis pathways. In this review, we discuss evidence for interplay between the UPS and protein-synthesis machinery, and outline the implications of this crosstalk for physiological and pathological processes in the CNS.
引用
收藏
页码:31 / 36
页数:6
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